The present invention relates to a process for the production of surface functionalised nanoparticles, particularly but not exclusively, the production of semiconductor quantum dot nanoparticles incorporating surface-bound functional groups which increase the ease with which the dots can be employed in applications, such as incorporation into solvents, inks, polymers, glasses, metals, electronic materials and devices, bio-molecules and cells.

The size of a semiconductor nanoparticle dictates the electronic properties of the material; the band gap energy being inversely proportional to the size of the semiconductor nanoparticle as a consequence of quantum confinement effects. In addition, the large surface area to volume ratio of the nanoparticle has a profound impact upon the physical and chemical properties of the nanoparticie.

Two fundamental factors, both related to the size of the individual semiconductor nanoparticle, are responsible for their unique properties. The first is the large surface to volume ratio; as a particle becomes smaller, the ratio of the number of surface atoms to those in the interior increases. This leads to the surface properties playing an important role in the overall properties of the material. The second factor being, with many materials including semiconductor nanoparticles, there is a change in the electronic properties of the material with size, moreover, because of quantum confinement effects the band gap gradually becomes larger as the size of the particle decreases. This effect is a consequence of the confinement of an 'electron in a box' giving rise to discrete energy levels similar to those observed in atoms and molecules, rather than a continuous band as observed in the corresponding bulk semiconductor material. Thus, for a semiconductor nanoparticle, because of the physical parameters, the "electron and hole", produced by the absorption of electromagnetic radiation, a photon, with energy greater then the first excitonic transition, are closer together than they would be in the corresponding macrocrystalline material, moreover the Coulombic interaction cannot be neglected. This leads to a narrow bandwidth emission, which is dependent upon the particle size and composition of the nanoparticle material. Thus, quantum dots have higher kinetic energy than the corresponding macrocrystalline material and consequently the first excitonic transition (band gap) increases in energy with decreasing particle diameter. Core semiconductor nanoparticles, which consist of a single semiconductor material along with an outer organic passivating layer, tend to have relatively low quantum efficiencies due to electron-hole recombination occurring at defects and dangling bonds situated on the nanoparticle surface which can lead to non-radiative electron-hole recombinations.

One method to eliminate defects and dangling bonds on the inorganic surface of the quantum dot is to grow a second inorganic material, having a wider band-gap and small lattice mismatch to that of the core material epitaxially on the surface of the core particle, to produce a "core-shell" particle. Core-shell particles separate any carriers confined in the core from surface states that would otherwise act as non-radiative recombination centres. One example is ZnS grown on the surface of CdSe cores.

Another approach is to prepare a core-multi shell structure where the "electron-hole" pair is completely confined to a single shell layer consisting of a few monolayers of a specific material such as a quantum dot-quantum well structure. Here, the core is of a wide bandgap material, followed by a thin shell of narrower bandgap material, and capped with a further wide bandgap layer, such as CdS/HgS/CdS grown using substitution of Hg for Cd on the surface of the core nanocrystal to deposit just a few monolayers of HgS which is then over grown by monolayers of CdS. The resulting structures exhibited clear confinement of photo-excited carriers in the HgS layer.

To add further stability to quantum dots and help to confine the electron-hole pair one of the most common approaches is by epitaxially growing a compositionally graded alloy layer on the core this can help to alleviate strain that could otherwise led to defects. Moreover, for a CdSe core, in order to improve structural stability and quantum yield, rather than growing a shell of ZnS directly on the core, a graded alloy layer of Cd _1-X Zn _x Se _1- yS _y can be used. This has been found to greatly enhance the photoluminescence emission of the quantum dots.

Doping quantum dots with atomic impurities is an efficient way also of manipulating the emission and absorption properties of the nanoparticle. Procedures for doping of wide band gap materials such as zinc selenide and zinc sulphide with manganese and copper (ZnSe:Mn or ZnSiCu), have been developed. Doping with different luminescence activators in a semiconducting nanocrystal can tune the photoluminescence and electroluminescence at energies even lower than the band gap of the bulk material, whereas the quantum size effect can tune the excitation energy with the size of the nanocrystals without causing a significant change in the energy of the activator related emission.

The coordination about the final inorganic surface atoms in any core, core-shell or core- multi shell, doped or graded nanoparticle is incomplete, with highly reactive, non-fully coordinated atoms "dangling bonds" on the surface of the particle, which can lead to particle agglomeration. This problem is overcome by passivating (also referred to as "capping") the "bare" surface atoms with protecting organic groups.

An outermost layer of organic material or sheath material (referred to as a "capping agent") helps to inhibit particle aggregation and protects the nanoparticles from their surrounding electronic and chemical environment. A schematic illustration of such a nanoparticle is provided in Figure 1. In many cases, the capping agent is the solvent in which the nanoparticle preparation is undertaken, and comprises a Lewis base compound or a Lewis base compound diluted in an inert solvent, such as a hydrocarbon. The lone pair of electrons on the Lewis base capping agent are capable of a donor-type coordination to the surface of the nanoparticles. Suitable Lewis base compounds include mono- or mulit- dentate ligands, such as phosphines (trioctylphosphine, triphenolphosphine, t- butylphosphine), phosphine oxides (trioctylphosphine oxide), alkyl phosphonic acids, alkyl- amines (hexadecylamine, octylamine), aryl-amines, pyridines, long chain fatty acids and thiophenes, but is not restricted to these materials.

The widespread exploitation of quantum dot nanoparticles has been restricted by their physical/chemical instability and incompatibility with many applications. In particular, the inability to find acceptable methods of incorporating nanoparticles into silicone polymers has severely limited the use of nanoparticles in electronic devices. Consequently, a series of surface modification procedures has been employed to render the quantum dots more stable and compatible with a desired application. This has been attempted mainly by making the capping agent bi- or multi functional or by overcoating the capping layer with an additional organic layer that has functional groups which can be used for further chemical linkage.

The most widely used quantum dot surface modification procedure is known as 'ligand exchange'. The ligand molecules that inadvertently coordinate to the surface of the quantum dot during the core synthesis and shelling procedure are subsequently exchanged with a ligand compound that introduces a desired property or functional group. Inherently, this ligand exchange strategy reduces the quantum yield of the quantum dots considerably. This process is illustrated schematically in Figure 2.

An alternative surface modification strategy interchelates discrete molecules or polymer with the ligand molecules that are already coordinated to the surface of the quantum dot during the shelling procedure. These post synthesis interchelation strategies often preserve the quantum yield but result in quantum dots of substantially larger size. This process is illustrated schematically in Figure 3.

Current ligand exchange and interchelation procedures may render the quantum dot nanoparticles more compatible with their desired application but usually results in lower quantum yield due to damage to the inorganic surface of the quantum dots and/or an increase in the size of the final nanoparticles. Moreover, an economically viable method for producing surface functionalised nanoparticles suitable for incorporation into silicone polymers has still to be realised.

It is an object of the present invention to obviate or mitigate one or more of the problems described above.

According to a first aspect of the present invention there is provided a method for producing surface functionalised nanoparticles for incorporation into a silicone polymer material, the method comprising reacting growing nanoparticles with a nanoparticle surface binding ligand incorporating a nanoparticle binding group and a silicone polymer binding group, said reaction being effected under conditions permitting binding of said surface binding ligand to the growing nanoparticles to produce said surface functionalised nanoparticles. The present invention provides a method for providing a functionalised layer on the outer surface of a nanoparticle which is suitable for binding to a silicone polymer. Even though this has seemingly proved difficult in the past, it has surprisingly been found that nanoparticles can in fact be combined with a pre-functionalised nanoparticle surface binding ligand containing a silicone polymer binding group without harming the ability of the surface binding ligand to bind to the surface of the nanoparticles of the ability of the other functional group to bind to a silicone polymer.

The present invention thus provides a strategy for intentionally coordinating a chosen pre- chemically functionalised ligand to the surface of a quantum dot nanoparticle in-situ and thereby generate quantum dot nanoparticles that are physically/chemically robust, have high quantum yield, have small diameter and, importantly are ready for incorporation into silicone polymers which then facilitates the use of such quantum dots in electronic devices such as LEDs.

Preferably the method comprises synthesising said growing nanoparticles in the nanoparticle surface binding ligand under conditions permitting binding of the surface binding ligand to the growing nanoparticles to produce said surface functionalised nanoparticles.

The present invention provides a method for producing surface functionalised nanoparticles for incorporation into a silicone polymer material, the method comprising synthesising nanoparticles in a nanoparticle surface binding ligand incorporating a nanoparticle binding group and a silicone polymer binding group under conditions permitting binding of said surface binding ligand to the growing nanoparticles during synthesis to produce said surface functionalised nanoparticles.

The present invention facilitates synthesis of nanoparticles in a capping agent that has a nanoparticle binding group which can passivate the surface of the nanoparticle and an additional ligand which has the ability for further chemical linkage, such as cross linking about the nanoparticle or incorporation within polymeric materials. The growing nanoparticles may be pre-formed nanoparticle cores on to which one or more shell layers are being grown in the presence of the nanoparticle surface binding ligand as in the Example set out below, or the growing nanoparticles may be growing nanoparticle cores produced by an appropriate combination of core precursor materials.

The Nanoparticles

In a first preferred embodiment of the method forming the first aspect of the present invention the nanoparticle contains a first ion and a second ion. The first and second ions may be selected from any desirable group of the periodic table, such as but not limited to group 11, 12, 13, 14, 15 or 16 of the periodic table. The first and/or second ion may be a transition metal ion or a d-block metal ion. Preferably the first ion is selected from group 11 , 12, 13 or 14 and the second ion is selected from group 14, 15 or 16 of the periodic table. Surface functionalised nanoparticles produced according to the first aspect of the present invention are preferably semiconductor nanoparticles, for example, core nanoparticles, core-shell nanoparticles, graded nanoparticles or core-multishell nanoparticles incorporating the desired surface functionalisation.

Suitable Solvents for use in the Method of the Present Invention

The reaction between the growing nanoparticles and the ligand may be carried out in any appropriate solvent. The reaction is preferably carried out in a solvent which is different to said nanoparticle surface binding ligand, although it will be appreciated that this does not have to be the case, and that in alternative embodiments the surface binding ligand may represent the solvent or one of the solvents in which the reaction is being conducted. The solvent may be a co-ordinating solvent (i.e. a solvent that co-ordinates the growing nanoparticles) or a non-co-ordinating solvent (i.e. a solvent that does not co-ordinate the growing nanoparticles). Preferably the solvent is a Lewis base compound, which may be selected from the group consisting of HDA, TOP, TOPO, DBS, octanol and the like.

The Nanoparticle Surface Binding Ligand

The nanoparticle binding group of the surface binding ligand is preferably different to the silicone binding group. The silicone binding group may or may not incorporate a protecting group chosen so as to be selectively removable. The nature of the silicone binding group of the surface binding ligand may be chosen to bestow any desirable chemical or physical property to the final surface functionalised nanoparticles provided it retains the ability to bind to a silicone polymer. For example, a ligand may be chosen which contains a silicone binding group which, in addition to enabling the bound nanoparticles to be incorporated into a silicone polymer, bestows the surface functionalised nanoparticles with a predetermined reactivity towards a particular reagent. Alternatively, a ligand may be chosen which incorporates a silicone binding group which bestows aqueous compatibility (i.e. the ability to be stably dispersed or dissolved in aqueous media) to the surface functionalised nanoparticles as well as the ability to crosslink with silicone polymers which incorporate compatible cross-linkable groups.

The surface binding ligand may contain any appropriate nanoparticle binding group to bind to the nanoparticles. Preferably the nanoparticle binding group contains an atom selected from the group consisting of sulfur, nitrogen, oxygen and phosphorous. The nanoparticle binding group may contain a species selected from the group consisting of a thio group, an amino group, an oxo group and a phospho group. The nanoparticle binding group may be selected from the group consisting of hydroxide, alkoxide, carboxylic acid, carboxylate ester, amine, nitro, polyethyleneglycol, sulfonic acid, sulfonate ester, phosphoric acid and phosphate ester. Moreover, the nanoparticle binding group may be a charged or polar group, such as but not limited to a hydroxide salt, alkoxide salt, carboxylate salt, ammonium salt, sulfonate salt or phosphate salt.

The nanoparticle binding group and the silicone polymer binding group of the surface binding ligand are preferably connected via a linker, which may take any desirable form. It is particularly preferred that said linker is selected from the group consisting of a covalent bond; a carbon, nitrogen, oxygen or sulfur atom; a substituted or unsubstituted, saturated or unsaturated aliphatic or alicyclic group; and a substituted or unsubstituted aromatic group.

The present invention provides methods for producing surface functionalised nanoparticles that can be incorporated into a silicone polymer and are also physically/chemically robust, have high quantum yield, have small diameter and are compatible with their intended application. Nanoparticles produced according to the present invention may be represented by Formula 1 below.

QD-X-Y-Z

Formula 1

Wherein: QD represents a core or core-(multi)shell nanoparticle; and X-Y-Z represents the nanoparticle surface binding ligand in which X is a nanoparticle surface binding group; Y is a linker group linking X and Z; and Z is a functional group which can bind to a silicone polymer.

X and/or Z may be substituted or unsubstituted alkyl, substituted or unsubstituted aryl, substituted or unsubstituted heterocyclic, substituted or unsubstituted polyethyleneglycol (examples of substituents include but are not limited to halogen, ether, amine, amide, ester, nitrile, isonitrile, aldehyde, carbonate, ketone, alcohol, carboxylic acid, azide, imine, enamine, anhydride, acid chloride, alkyne, thiol, sulfide, sulfone, sulfoxide, phosphine, phosphine oxide).

X and/or Z may be a charged or polar group, such as a hydroxide salt, alkoxide salt, carboxylate salt, ammonium salt, sulfonate salt or phosphate salt.

X and/or Z may be selected from the group consisting of: -SR ¹ (R ¹ = H, alkyl, aryl); -OR ² (R ² - H, alkyl, aryl); -NR ³ R ⁴ (R ³ and/or R ⁴ = H, alkyl, aryl); -CO ₂ R ⁵ (R ⁵ = H, alkyl, aryl); - P(=O)OR ⁶ OR ⁷ (R ⁶ and/or R ⁷ = H, alkyl, aryl); -OR ⁸ wherein R ⁸ is hydrogen or an alkyl group which may be substituted or unsubstituted, and/or saturated or unsaturated; - C(O)OR ⁹ wherein R ⁹ is hydrogen, a substituted or unsubstituted, saturated or unsaturated aliphatic or alicyclic group, or a substituted or unsubstituted aromatic group; -NR ¹⁰ R ¹¹ wherein R ¹⁰ and R ¹¹ are independently hydrogen, a substituted or unsubstituted, saturated or unsaturated aliphatic or alicyclic group, or a substituted or unsubstituted aromatic group, or R ¹⁰ and R ¹¹ may be linked such that -NR ¹⁰ R ¹¹ forms a nitrogen-containing heterocyclic ring of any desirable size, e.g. a five, six or seven-membered ring; -N ⁺ R ¹² R ¹³ R ¹⁴ wherein R ¹² , R ¹³ and R ¹⁴ are independently hydrogen, a substituted or unsubstituted, saturated or unsaturated aliphatic or alicyclic group, or a substituted or unsubstituted aromatic group; - NO ₂ ; -(-OCH ₂ CH ₂ V-OR ¹⁵ wherein R ¹⁵ is hydrogen, a substituted or unsubstituted, saturated or unsaturated aliphatic or alicyclic group, or a substituted or unsubstituted aromatic group; -S(O) ₂ OR ¹⁶ wherein R ¹⁶ is hydrogen, a substituted or unsubstituted, saturated or unsaturated aliphatic or alicyclic group, or a substituted or unsubstituted aromatic group; and -P(OR ¹⁷ )(OR ¹⁸ )O wherein R ¹⁷ and R ¹⁸ are independently hydrogen, a substituted or unsubstituted, saturated or unsaturated aliphatic or alicyclic group, or a substituted or unsubstituted aromatic group.

Z may incorporate any appropriate protecting group. By way of example, Z may contain an acid labile protecting group, such as f-butyl, benzylic, trityl, silyl, benzoyl, fluorenyl, acetal, ester, or ethers, e.g. methoxymethyl ether, 2-methoxy(ethoxy)methyl ether. Alternatively, Z may contain a nucleophillic-base labile protecting group, including a carboxylic ester, sulfonium salt, amide, imide, carbamate, Λ/-sulfonamide, trichloroethoxymethyl ether, trichloroethylester, trichloroethoxycarbonyl, allylic-ether / amine / acetal / carbonate / ester / carbamate to protect a carboxylic acid, alcohol, thiol etc. Moreover, Z may incorporate a benzyl amine protecting group, which can be deprotected to provide an amine group, or Z may contain a cyclic carbonate when it is ultimately desirable to deprotect Z to provide a diol for further reaction.

Y may be a single bond, alkyl, aryl, heterocyclic, polyethyleneglycol, substituted or unsubstituted alkyl, substituted or unsubstituted aryl, substituted or unsubstituted ^' heterocyclic, substituted or unsubstituted polyethyleneglycol, (examples of substituents include halogen, ether, amine, amide, ester, nitrile, isonitrile, aldehyde, carbonate, ketone, alcohol, carboxylic acid, azide, imine, enamine, anhydride, acid chloride, alkyne, thiol, sulfide, sulfone, sulfoxide, phosphine, phosphine oxide), a crosslinkable/polymerisable group (examples include carboxylic acid, amine, vinyl, alkoxysilane, epoxide), or a group represented by Formula 2 below Formula 2

Wherein: k, m and n are each independently any number from O to around 10,000. X and/or Z may be the same or different. X may be any of the groups specified above in respect of the nanoparticle binding group, for example X may be an acid group or an ester group, such as a carboxylic acid group or derivative or salt thereof, such as a carboxylate ester or carboxylate salt. In alternative embodiments, X may be a sulfonic acid group, sulfonate ester or salt; or a phosphoric acid group, phosphate ester or salt; or an amino group. Z preferably comprises one or more alkyl group, each containing at least one unsaturated group for connection to the silicone polymer. The or each carbon-to-carbon double or triple bond may be a terminal unsaturated group (i.e. include an atom at the end of a carbon chain) or be provided within the carbon chain. Where Z comprises one or more alkyl groups, the or each alkyl chain may carry any desirable substituent(s). The linker group, Y, connecting X and Z may take any convenient form. For example, Y may contain one or more aliphatic groups and/or an aromatic groups. The aliphatic group(s) may contain a straight carbon chain, a branched carbon chain, or may be alicyclic. Y may further comprise one or more ether groups. In particularly preferred embodiment, Y comprises a phenyl group bound to at least one, more preferably two or three, unsaturated alkyl groups optionally via ether links. A particularly preferred nanoparticle surface binding ligand (Ligand 1) has the structure shown below, which can cross-link to other ligands and/or surrounding species (e.g. compatible polymers or polymerizable monomers) via the three vinyl groups.

Ligand i

Further preferred cross-linkable ligands of Formula 1 which can be used in the method according to the present invention are shown below and incorporate a functional group, Z, which contains one or more vinyl groups bonded to an aliphatic or aromatic linker, Y, which is bonded to a nanoparticle binding ligand, X, of any desirable structure, such as those described above. Preferred ligands incorporate one vinyl group, more preferably two vinyl groups, and most preferably three or more vinyl groups. Where Z contains two or more vinyl groups, then the vinyl groups may be bonded via respective alkyl groups to the same carbon atom, or to different carbon atoms (e.g. different carbon atoms of the same carbocyclic or heterocyclic ring, which may itself be saturated, partially saturated or aromatic). Nanoparticle binding group, X, may be monodentate or multidentate as described above. By way of example, X may incorporate one carboxylic acid group, as in Ligand 1., or X may incorporate two, three or more carboxylic acid groups. Where two or more carboxylic acid groups are present, each group may be bonded via an alkyl group to the same or different carbon atoms.

Exemplary monodentate aliphatic ligands include the following, wherein X is a carboxylic acid group, Z comprises one, two or three vinyl groups, Y is a straight or branched aliphatic group, and each x is any integer (i.e. 0, 1, 2, 3 etc).

Exemplary monodentate aromatic ligands include the following, wherein X is a carboxylic acid group, Z comprises one, two or three vinyl groups, Y contains an aromatic group, and each x is any integer (i.e. 0, 1 , 2, 3 etc).

Exemplary bidentate aliphatic ligands include the following, wherein X contains two carboxylic acid groups, Z comprises one, two or three vinyl groups, Y is a straight or branched aliphatic group, and each x is any integer (i.e. 0, 1 , 2, 3 etc).

Exemplary tridentate aliphatic ligands include the following, wherein X contains three carboxylic acid groups, Z comprises one, two or three vinyl groups, Y is a straight or branched aliphatic group, and each x is any integer (i.e. O, 1 , 2, 3 etc).

It will be appreciated that one or more of the carboxylic acid groups in any of the above exemplary structures may be replaced with an alternative nanoparticle binding group, such as, but not limited to, a carboxylic acid salt or ester, a sulfonic acid, ester or salt, a phosphoric acid, ester or salt, or an amino group. Moreover, linker group, Y, may contain groups other than the specific unsaturated aliphatic or aromatic groups shown above. For example, Y may incorporate one or more ether groups, carbon-to-carbon double bonds, and/or multicyclic aromatic or non-aromatic groups.

In a preferred embodiment there is provided a method according to the first aspect of the present invention, wherein the nanoparticle surface binding ligand incorporates a terminal unsaturated group in the form of a vinyl group. That is, the nanoparticle surface binding ligand incorporates a carbon-to-carbon double bond at the end of the ligand furthest away from the nanoparticle surface.

X may comprise at least one carboxylic acid group or at least one thiol group. Y may comprise a straight or branched aliphatic group, or an aromatic group.

With regard to the first aspect of the present invention the nanoparticle surface binding ligand may be poly(oxyethylene glycol) _n monomethyl ether acetic acid wherein n = around 1 to around 5000. Preferably n is around 50 to 3000, more preferably around 250 to 2000, and most preferably around 350 to 1000. Alternatively, the nanoparticle surface binding ligand may be selected from the group consisting of 10-Undecylenic acid and 11- mercapto-undecene. As a further preferred alternative, the nanoparticle surface binding ligand is Ligand 1. as shown above. .

Surface Functionalised Nanoparticles

A second aspect of the present invention provides a surface functionalised nanoparticle produced using the method according to the first aspect of the present invention, said surface functionalised nanoparticle comprising a nanoparticle bound to a nanoparticle surface binding ligand, said ligand incorporating a nanoparticle binding group and a silicone polymer binding group.

Nanoparticles produced according to the first aspect of the present invention are preferably semiconductor nanoparticles, for example, core nanoparticles, core-shell nanoparticles, graded nanoparticles or core-multishell nanoparticles. Said nanoparticles preferably comprise one or more ions selected from any suitable group of the periodic table, such as but not limited to group 11, 12, 13, 14, 15 or 16 of the periodic table, transition metal ions and/or d-block metal ions. The nanoparticle core and/or shell (where applicable) may incorporate one or more semiconductor material selected from the group consisting of CdS, CdSe, CdTe, ZnS, ZnSe, ZnTe, InP, InAs, InSb, AIP, AIS, AIAs, AISb, GaN, GaP, GaAs, GaSb, PbS, PbSe, Si, Ge, MgS, MgSe, MgTe and combinations thereof.

The present invention describes a strategy that intentionally coordinates a chosen pre- chemically functionalised ligand to the surface of the quantum dot nanoparticle in-situ and generates quantum dot nanoparticles that are physically/chemically robust, have high quantum yield, have small diameter and which can be incorporated into silicone polymers, which can subsequently be employed in the production of electronic devices, such as LEDs.

The present invention is illustrated with reference to the following non-limiting Example and Figures in which,

Figure 1 is a schematic illustration of a prior art core-shell quantum dot nanoparticle incorporating an interchelated surface ligand;

Figure 2 is a schematic illustration of the prior art process of ligand exchange; and

Figure 3 is a schematic illustration of the prior art process of ligand interchelation.

EXAMPLE

InP core nanoparticle quantum dots were initially prepared using a molecular cluster compound to seed nanoparticle growth according to the invention described in the applicant's co-pending European patent application, EP1743054A.

A shell of ZnS was then deposited on the InP cores employing Ligand 1 as a capping agent.

Ligand i

Ligand 1 was produced according to the reaction scheme shown below.

To produce the InP/ZnS core-shell nanoparticles, a flame dried three-necked flask (10OmL), equipped with a condenser with a side arm, a thermometer, a suba seal and a stirrer bar was initially charged with indium phosphide core nanoparticles (0.155 g in 4.4 mL dibutyl sebacate) and degassed at 100 ⁰ C for 1 hour. The flask was allowed to cool to room temperature and then back filled with nitrogen. Zinc acetate (0.7483 g) and Ligand \ (0.5243 g) was then added, the mixture degassed at 55 ⁰ C for 1 hour and backfilled with nitrogen. The reaction temperature was increased to 190 ⁰ C, terf-nonyl mercaptan (0.29 mL) was added dropwise, the temperature increased to 190 ⁰ C and held for 1 hour and 30 minutes. The temperature was decreased to 180 °C, 1-octanol (0.39 ml_) added and the temperature held for 30 minutes. The reaction mixture was cooled to room temperature.

InP/ZnS core-sheli nanoparticles particles were isolated under N ₂ in ethyl acetate by centrifugation. The particles were precipitated with acetonitrile followed by centrifugation. The particles were dispersed in chloroform and re-precipited with acetonitrile followed by centrifugation. This dispersion-precipitation procedure using chloroform and acetonitrile was repeated four times in total. The InP/ZnS core-shell particles were finally dispersed in chloroform.

The resulting core-multishell nanoparticles coated with Ligand 1 _, as the capping agent may then be treated with a Hoveyda-Grubbs catalyst under standard conditions to cross-link adjacent terminal vinyl groups as shown in the exemplary reaction scheme below.

Hoveyda-Grubbs Catalyst

Alternatively, the terminal vinyl groups of Ligand 1 could be cross-linked before coordination to the nanoparticles as shown below.

Either before of after cross-linking the surface binding ligand the surface functionalised nanoparticles can then be incorporated into silicone based materials employing the methodology outlined in the reaction scheme below (x and y represent the number of repeating units of each silicone containing species).

Pt-complex